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KENYATAAN MEDIA : PENGUMUMAN PERANTI PERUBATAN TIDAK BERDAFTAR GAUZE PACK WITH X-RAY DETECTABLE LINE JENAMA WHITE DOVE 09 Mac 2023 7184
FIRST EDITION GUIDANCE DOCUMENT MDA/GD/0064: NOTIFICATION OF CUSTOM-MADE MEDICAL DEVICES 01 Mac 2023 5874
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NEW RELEASE GUIDELINE DOCUMENT MDA/GL/10: GUIDELINE DOCUMENT ON HOW TO SUBMIT AN APPLICATION FOR REGISTRATION OF A REFURBISHED MEDICAL DEVICE 11 Januari 2023 7950
Fifth Edition Guideline for Medical Device-Drug and Drug-Medical Device Combination Product 11 Januari 2023 7937
PUBLIC COMMENT DRAFT GUIDANCE DOCUMENT REQUIREMENTS FOR APPLICATION OF CERTIFICATE OF FREE SALE (CFS), MANUFACTURING CERTIFICATE (MC) AND CERTIFICATE OF FREE SALE FOR EXPORT ONLY (CFS EO) MEDICAL DEVICES 23 Disember 2022 7792
REGISTRATION OF COVID-19 TEST KITS THAT HAVE BEEN APPLIED VIA CONDITIONAL APPROVAL AND SPECIAL ACCESS 16 Disember 2022 7219
How Do I Keep Up with The Latest Regulatory Information and Activities? - Medical Device Authority-Regulatory Information 14 Disember 2022 11319

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